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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-Pyrrolidineacetic acid, 1-[(1,1-dimethylethoxy)carbonyl]-

OC(=O)CC1CCCN1C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 2-Pyrrolidineacetic acid, 1-[(1,1-dimethylethoxy)carbonyl]-
CAS Number: 194154-91-1
Product Number: AG0074OY(AGN-PC-0BX30P)
Synonyms:
MDL No:
Molecular Formula: C11H19NO4
Molecular Weight: 229.2729

Identification/Properties

Computed Properties
Molecular Weight:
229.276g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
229.131g/mol
Monoisotopic Mass:
229.131g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
282
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
2811
Hazard Statements:
H301-H410
Precautionary Statements:
P273-P301+P310-P305+P351+P338
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 2-(1-(tert-Butoxycarbonyl)pyrrolidin-2-yl)acetic acid plays a crucial role in chemical synthesis as a versatile building block. Its unique structure containing a pyrrolidine ring and a carboxylic acid group allows for diverse functionalization and reactivity in various synthetic pathways. This compound is commonly employed as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other valuable organic compounds. Its presence enables the introduction of both the pyrrolidine moiety and the acetic acid functionality into target molecules, facilitating the creation of novel compounds with desired properties and biological activities. Additionally, the tert-butoxycarbonyl protecting group on the pyrrolidine nitrogen enhances the compound's stability and selectivity during reactions, making it a valuable tool in organic chemistry.